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Clinical trials for 2012-000214-11

The European Union Clinical Trials Register   allows you to search for protocol and results information on:
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    The EU Clinical Trials Register currently displays   44365   clinical trials with a EudraCT protocol, of which   7389   are clinical trials conducted with subjects less than 18 years old.   The register also displays information on   18700   older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).

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    1 result(s) found for: 2012-000214-11. Displaying page 1 of 1.
    EudraCT Number: 2012-000214-11 Sponsor Protocol Number: RG_11-225 Start Date*: 2013-06-18
    Sponsor Name:University of Birmingham
    Full Title: BREVITY: A phase II study of brentuximab vedotin using a response adapted design in patients with Hodgkin lymphoma unsuitable for chemotherapy due to age, frailty or co-morbidity
    Medical condition: Hodgkin lymphoma
    Disease: Version SOC Term Classification Code Term Level
    16.1 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) 10020261 Hodgkin's disease NOS stage II LLT
    16.1 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) 10020270 Hodgkin's disease stage III PT
    16.1 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) 10020269 Hodgkin's disease stage II PT
    16.1 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) 10061597 Hodgkin's disease stage IV PT
    16.1 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) 10020265 Hodgkin's disease NOS stage IV LLT
    16.1 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) 10020264 Hodgkin's disease NOS stage III LLT
    Population Age: Adolescents, Under 18, Adults, Elderly Gender: Male, Female
    Trial protocol: GB (Completed)
    Trial results: View results
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    The status and protocol content of GB trials is no longer updated since 1 January 2021. For the UK, as of 31 January 2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI. Legal notice
    As of 31 January 2023, all EU/EEA initial clinical trial applications must be submitted through CTIS . Updated EudraCT trials information and information on PIP/Art 46 trials conducted exclusively in third countries continues to be submitted through EudraCT and published on this website.

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